Documentation and qualification
Everything at a glance – our documentation includes technical operation manuals with layouts, schemata, parts lists, and remaining risks.
Failure mode and effects analysis (FMEA) allows us to avoid errors from the outset rather than discovering and correcting them later on. The later an error is discovered, the more difficult and expensive it is to correct. That is why we carry out this analysis during the development phase.
GMP and GAMP standards
When it comes to robotics solutions, we know how important compliance is – and that is why we place so much value on the documentation and validation (IQ/OQ/PQ) of our systems. We strictly comply with the good manufacturing practice and good automated manufacturing practice standards (GMP and GAMP).
In addition to internal analyses, we also carry out partial or complete conformity assessments for every system. All of our systems are subject to comprehensive testing in accordance with the CE guidelines.